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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118830Generated: November 1, 2026

Water → (Z)-2-Methoxyimino-3-oxobutyric acid, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/2118830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178468383HCID 178468383—
SolventAcetoneHCID 180—
Product(Z)-2-Methoxyimino-3-oxobutyric acid, 1,1-dimethylethyl esterHCID 6420338—

Reaction Conditions

Temperature5 °C

Reaction Steps

626.65 g of (Z)-2-hydroxyimino-3-oxo-butyric acid tert.butyl ester are dissolved in 2.86 l of acetone. The solution is cooled to 5° C. and treated portionwise with 703.5 g of potassium carbonate. 322 ml of dimethyl sulphate are then added dropwise to the yellow suspension without cooling during 1 hour, whereby the temperature of the mixture should not rise above 25° C. The light beige suspension is stirred at 20°-25° C. for about 4 hours until starting material can no longer be detected by thin-layer chromatography. Thereafter, the mixture is poured into 7 l of water and extracted three times with 1 l of ethyl acetate each time. The combined ethyl acetate extracts are washed three times with 1 l of water each time, dried over sodium sulphate and evaporated in vacuo at 40° C. The residual yellow oil is dried for a further 6 hours in a high vacuum at 40° C. and subsequently distilled. There is obtained (Z)-2-methoxyimino-3-oxo-butyric acid tert.butyl ester as a yellow oil with a boiling point of 57° C. at 0.02 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04680408
Source datasetuspto-grants-1987_07
ORD IDord-a989a217b54b41a9a81c732a93cea126
Source noteuspto-grants-1987_07